Master-Dent 60-200
Master-Dent 60-200 is a device made by Dentonics, Inc., cleared under FDA 510(k) K041886 on 4 Aug 2004 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00816526020343), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816526020343 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK041886 | Date4 Aug 2004 | StatusActive |
Official records
- AccessGUDID record 00816526020343
- FDA 510(k) database K041886
Across registries
- FDA 510(k) K041886 decided 4 Aug 2004 Active
- FDA GUDID UDI-DI 00816526020343 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K041886
- Listed FDA GUDID 00816526020343
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Master-Dent
- Generic name
- Temporary dental crown/bridge
- Model / reference
- 60-200
- Description
- Temporary Crown and Bridge Material, Shade A2 1 X 50ml Cartridge w/ Tips
- Primary DI / UDI-DI
- 00816526020343
- 510(k) Number
- GMDN term
- Temporary dental crown/bridge
- GUDID distribution status
- In Commercial Distribution